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P021

Peptide 021, GLXC-21260

A tetrapeptide derived from CNTF, designed to promote neurogenesis, enhance cognition, and mitigate Alzheimer's pathologies by modulating neurotrophic signaling.

Quick Stats
Studies 37
Trials 57
Formula C27H42N6O8
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Utility 2
pubmed 2005

Role of the beta-adrenergic receptor kinase in myocardial dysfunction after brain death.

Pandalai. Prakash K PK; Lyons. Jefferson M JM; Duffy. Jodie Y JY; McLean. Kelly M KM; Wagner. Connie...

In a pig study, causing brain death quickly turned off the heart's beta‑adrenergic receptors, making the heart pump less well. This happened because an enzyme called beta‑adrenergic receptor kinase (GRK) jumped up three‑fold, even though the number of receptors stayed the same.

Utility 2
pubmed Apr 3, 2017

Early neurotrophic pharmacotherapy rescues developmental delay and Alzheimer's-like memory deficits in the Ts65Dn mouse model of Down syndrome.

Kazim. Syed Faraz SF; Blanchard. Julie J; Bianchi. Riccardo R; Iqbal. Khalid K

In a mouse model of Down syndrome, giving a CNTF‑like peptide called P021 from before birth through early life fixed slow growth and later memory problems that look like early Alzheimer’s. The treatment also improved several brain proteins linked to learning and reduced a harmful enzyme activity. While the work is in mice, it hints that early neuro‑trophic support might help brain development and later cognition in Down syndrome.

Utility 1
pubmed Jul 24, 2019

The frequency of SMN gene variants lacking exon 7 and 8 is highly population dependent.

Vijzelaar. Raymon R; Snetselaar. Reinier R; Clausen. Martijn M; Mason. Amanda G AG; Rinsma. Marrit M...

This study looked at how common a specific SMN gene deletion (missing exons 7 and 8) is in different ethnic groups. It found the deletion is fairly common in some European groups (up to 20%) but almost absent in Asian and African groups. The overall number of SMN gene copies stays about the same across populations.

Utility 1
pubmed Dec 20, 2005

Influence of obesity on timing of puberty.

Biro. Frank M FM; Khoury. Philip P; Morrison. John A JA

The study shows that higher body fat in kids tends to make girls start puberty earlier, while boys with less body fat may hit puberty sooner. Over the past decades, kids are hitting puberty earlier, likely because of more calories, fast food, less exercise, and more screen time. Early puberty can increase risks for metabolic problems later in life.

Utility 1
pubmed Jan 15, 1992

Increased growth of NIH/3T3 cells by transfection with human p120 complementary DNA and inhibition by a p120 antisense construct.

Perlaky. L L; Valdez. B C BC; Busch. R K RK; Larson. R G RG; Jhiang. S M SM; Zhang. W W WW; Brattain...

Scientists put a human protein called p120 into mouse cells and saw the cells turn cancer‑like and grow fast. When they added a matching antisense piece (p021) that blocks p120, the cells grew slower and looked normal again. This shows p120 can drive cell growth, and blocking it can reverse that effect, but the work was done in cell cultures and mice, not people.

Utility 1
pubmed Jan 1, 2013

Postnatal development of brain-derived neurotrophic factor (BDNF) and tyrosine protein kinase B (TrkB) receptor immunoreactivity in multiple brain stem respiratory-related nuclei of the rat.

Liu. Qiuli Q; Wong-Riley. Margaret T T MT

In baby rats, the brain chemicals BDNF and its receptor TrkB drop sharply around day 12 in brain areas that control breathing, which may explain why their response to low oxygen is weakest then. The levels bounce back by day 14, and other brain regions show different patterns of change.

Utility 1
pubmed Sep 2, 2019

C<sub>2</sub>-Ceramide-Induced Rb-Dominant Senescence-Like Phenotype Leads to Human Breast Cancer MCF-7 Escape from <i>p</i>53-Dependent Cell Death.

Chang. Wen-Tsan WT; Wu. Chang-Yi CY; Lin. Yin-Chieh YC; Wu. Min-Tsui MT; Su. Kai-Li KL; Yuan. Shyng-...

The study showed that a lab‑made form of ceramide can kill breast cancer cells with a broken p53 gene, but in cells with normal p53 it triggers a senescence‑like state that lets them avoid death. This means ceramide’s effects vary by cell type and can sometimes protect cancer cells rather than destroy them.

Utility 1
pubmed 2002

Age-dependency of analgesia elicited by intraoral sucrose in acute and persistent pain models.

Anseloni. Vanessa C Z VC; Weng. H-R HR; Terayama. R R; Letizia. David D; Davis. Barry J BJ; Ren. Ke...

In baby rats, giving a sweet sugar solution by mouth can temporarily dull pain from heat or pressure, but this effect only shows up in the first few weeks after birth and disappears by about three weeks old. The pain‑relief works a bit better when the rats have inflamed paws, and the timing of the effect differs slightly between front and back paws.

Utility 1
pubmed Dec 21, 2023

Tau and Alzheimer's disease: Past, present and future.

Iqbal. Khalid K

The paper explains that a protein called tau becomes abnormal in Alzheimer's and other brain diseases, forming tangled clumps that damage nerve cells. Scientists are trying to treat this by making vaccines or antibodies that target tau, but the early human trials have shown mixed results and no clear cure yet.

pubmed Nov 21, 2024

Candidate serum protein biomarkers for active pulmonary tuberculosis diagnosis in tuberculosis endemic settings.

Ayalew. Sosina S; Wegayehu. Teklu T; Wondale. Biniam B; Tarekegn. Azeb A; Tessema. Bamlak B; Admasu....

Researchers found a set of eight proteins in blood that can accurately tell if someone has active lung TB, even when other lung issues are present. This could lead to a simple blood test for TB, but it doesn’t change everyday health hacks or performance strategies.

pubmed Mar 11, 2024

Optimized MLPA workflow for spinal muscular atrophy diagnosis: identification of a novel variant, NC_000005.10:g.(70919941_70927324)del in isolated exon 1 of SMN1 gene through long-range PCR.

Yao. Mei M; Jiang. Liya L; Yu. Yicheng Y; Cui. Yiqin Y; Chen. Yuwei Y; Zhou. Dongming D; Gao. Feng F...

Scientists improved a lab test to spot a rare genetic change that causes spinal muscular atrophy, finding a new 7.3 kb deletion in the SMN1 gene that appears in two unrelated Chinese families.

pubmed Feb 10, 2015

[Analysis of SMN1 gene partial deletion of spinal muscular atrophy based on MLPA].

Zhang. Wenhui W; Cao. Yanyan Y; Song. Fang F; Qu. Yujin Y; Bai. Jinli J; Jin. Yuwei Y; Wang. Hong H

Researchers used a DNA test called MLPA to look at seven people with suspected spinal muscular atrophy and found two different patterns of small deletions in the SMN1 gene. Both patterns always removed exon 7, which is the key piece that causes the disease, and these tiny deletions would have been missed by older testing methods.

pubmed Dec 10, 2019

[Supplementary value of denaturing high performance liquid chromatography for routine prenatal diagnosis of spinal muscular atrophy by multiple ligation-dependent probe amplification].

Tan. Yujie Y; Wang. Hao H; Zhao. Taikun T; Cheng. Ming M; Zhang. Chan C

The researchers showed that using a lab technique called DHPLC together with another test (MLPA) can reliably find carriers of spinal muscular atrophy (SMA) and correctly diagnose whether a fetus has the disease. This is a diagnostic method for prenatal testing, not a treatment or health‑boosting strategy.

pubmed Mar 13, 2024

Variants located in intron 6 of <i>SMN1</i> lead to misdiagnosis in genetic detection and screening for SMA.

Qu. Yujin Y; Bai. Jinli J; Jiao. Hui H; Qi. Hong H; Huang. Wenchen W; OuYang. Shijia S; Peng. Xiaoyi...

The study shows that certain DNA changes inside the SMN1 gene can trick standard genetic tests into wrongly saying a person has two missing copies of the gene, which could lead to a misdiagnosis of spinal muscular atrophy. Using a different test (MLPA‑P021) or sequencing avoids this error.